geneid | 1829 |
---|---|
ensemblid | ENSG00000046604.14 |
hgncid | 3049 |
symbol | DSG2 |
name | desmoglein 2 |
refseq_nuc | NM_001943.5 |
refseq_prot | NP_001934.2 |
ensembl_nuc | ENST00000261590.13 |
ensembl_prot | ENSP00000261590.8 |
mane_status | MANE Select |
chr | chr18 |
start | 31498177 |
end | 31549008 |
strand | + |
ver | v1.2 |
region | chr18:31498177-31549008 |
region5000 | chr18:31493177-31554008 |
regionname0 | DSG2_chr18_31498177_31549008 |
regionname5000 | DSG2_chr18_31493177_31554008 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1118 | 220 | 80 | 36 | 79 | 6 | 18 | 55 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002 | 0/1 | 1118 | 104 | 5 | 16 | 64 | 5 | 13 | 45 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0003 | 0/0 | 1118 | 8 | 0 | 6 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0004 | 0/0 | 1118 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0005 | 0/0 | 1118 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0006 | 0/0 | 1118 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0007 | 0/0 | 1118 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0008 | 0/0 | 1118 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0009 | 0/0 | 1118 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0010 | 0/0 | 1118 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0011 | 0/0 | 1118 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0012 | 0/0 | 1118 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0013 | 0/0 | 1118 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0014 | 0/0 | 1118 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3357 | 98 | 10 | 26 | 42 | 5 | 14 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0002 | 0/1 | 3357 | 79 | 5 | 16 | 43 | 5 | 9 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0003 | 0/0 | 3357 | 72 | 32 | 4 | 31 | 1 | 4 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0004 | 0/0 | 3357 | 22 | 0 | 0 | 21 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0005 | 0/0 | 3357 | 17 | 17 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0006 | 0/0 | 3357 | 15 | 13 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0007 | 0/0 | 3357 | 8 | 0 | 6 | 0 | 2 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0008 | 0/0 | 3357 | 6 | 0 | 0 | 6 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0009 | 0/0 | 3357 | 6 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0010 | 0/0 | 3357 | 5 | 4 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0011 | 0/0 | 3357 | 3 | 0 | 3 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0012 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0013 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0014 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0015 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0016 | 0/0 | 3357 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0017 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0018 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0019 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0020 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0021 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0022 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0023 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0024 | 0/0 | 3357 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0025 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0026 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
c0027 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2341 | 119 | 31 | 26 | 40 | 6 | 15 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0002 | 0/1 | 2343 | 114 | 5 | 22 | 70 | 7 | 9 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0003 | 0/0 | 2340 | 42 | 11 | 5 | 26 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0004 | 0/0 | 2342 | 36 | 17 | 3 | 11 | 1 | 4 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0005 | 0/0 | 2340 | 7 | 7 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0006 | 0/0 | 2343 | 7 | 5 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0007 | 0/0 | 2346 | 5 | 4 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0008 | 0/0 | 2340 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0009 | 0/0 | 2339 | 3 | 0 | 0 | 3 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0010 | 0/0 | 2343 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0011 | 0/0 | 2339 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0012 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0013 | 0/0 | 2339 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0014 | 0/0 | 2343 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0015 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0016 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0017 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0018 | 0/0 | 2341 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0019 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0020 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0021 | 0/0 | 2339 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
t0022 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 3 | 4 | 1 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0002 | 0/1 | 7 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0004 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3357 | 98 | 10 | 26 | 42 | 5 | 14 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0003 | 0/0 | 3357 | 72 | 32 | 4 | 31 | 1 | 4 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0005 | 0/0 | 3357 | 17 | 17 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0006 | 0/0 | 3357 | 15 | 13 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0008 | 0/0 | 3357 | 6 | 0 | 0 | 6 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0010 | 0/0 | 3357 | 5 | 4 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0011 | 0/0 | 3357 | 3 | 0 | 3 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0014 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0023 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0025 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0002 | 0/1 | 3357 | 79 | 5 | 16 | 43 | 5 | 9 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0004 | 0/0 | 3357 | 22 | 0 | 0 | 21 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0016 | 0/0 | 3357 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0027 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0003c0007 | 0/0 | 3357 | 8 | 0 | 6 | 0 | 2 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0004c0009 | 0/0 | 3357 | 6 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0005c0012 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0005c0021 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0006c0013 | 0/0 | 3357 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0007c0015 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0008c0022 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0009c0024 | 0/0 | 3357 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0010c0017 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0011c0018 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0012c0019 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0013c0026 | 0/0 | 3357 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0014c0020 | 0/0 | 3357 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5697 | 95 | 10 | 26 | 39 | 5 | 14 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0001t0009 | 0/0 | 5695 | 3 | 0 | 0 | 3 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0003t0003 | 0/0 | 5696 | 33 | 11 | 1 | 21 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0003t0004 | 0/0 | 5698 | 34 | 16 | 3 | 10 | 1 | 4 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0003t0008 | 0/0 | 5696 | 3 | 3 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0003t0015 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0003t0016 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0005t0001 | 0/0 | 5697 | 17 | 17 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0006t0005 | 0/0 | 5696 | 6 | 6 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0006t0006 | 0/0 | 5699 | 6 | 4 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0006t0017 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0006t0020 | 0/0 | 5702 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0006t0021 | 0/0 | 5695 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0008t0002 | 0/0 | 5699 | 6 | 0 | 0 | 6 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0010t0007 | 0/0 | 5702 | 5 | 4 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0011t0003 | 0/0 | 5696 | 3 | 0 | 3 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0014t0001 | 0/0 | 5697 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0023t0004 | 0/0 | 5698 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0001c0025t0001 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0002t0002 | 0/1 | 5699 | 77 | 5 | 16 | 43 | 5 | 7 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0002t0014 | 0/0 | 5699 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0004t0002 | 0/0 | 5699 | 22 | 0 | 0 | 21 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0016t0010 | 0/0 | 5699 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0002c0027t0002 | 0/0 | 5699 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0003c0007t0002 | 0/0 | 5699 | 8 | 0 | 6 | 0 | 2 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0004c0009t0003 | 0/0 | 5696 | 6 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0005c0012t0006 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0005c0012t0013 | 0/0 | 5695 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0005c0021t0019 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0006c0013t0012 | 0/0 | 5699 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0006c0013t0022 | 0/0 | 5699 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0007c0015t0011 | 0/0 | 5695 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0008c0022t0004 | 0/0 | 5698 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0009c0024t0018 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0010c0017t0001 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0011c0018t0001 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0012c0019t0001 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0013c0026t0005 | 0/0 | 5696 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
a0014c0020t0001 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | copy fasta | chr18 | 31493177 | 31554008 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 3 | 4 | 1 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0009g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0004 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0003t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0006g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0020g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0006t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0008t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0008t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0008t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0008t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0008t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0008t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0010t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0010t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0010t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0010t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0010t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0011t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0011t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0011t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0014t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0014t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0023t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0001c0025t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0002 | 0/1 | 7 | 0 | 1 | 5 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0014g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0002t0014g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0016t0010g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0002c0027t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0003c0007t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0004c0009t0003g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0004c0009t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0004c0009t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0004c0009t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0005c0012t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0005c0012t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0005c0012t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0005c0021t0019g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0006c0013t0012g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0006c0013t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0007c0015t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0007c0015t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0008c0022t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0009c0024t0018g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0010c0017t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0011c0018t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0012c0019t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0013c0026t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
a0014c0020t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0002 | g0021 | EUR | GBR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00140 | hp2 | a0001 | c0003 | t0004 | g0031 | EUR | GBR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0069 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00280 | hp2 | a0003 | c0007 | t0002 | g0067 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | FIN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00423 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00438 | hp1 | a0002 | c0004 | t0002 | g0016 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00544 | hp1 | a0012 | c0019 | t0001 | g0270 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00544 | hp2 | a0001 | c0003 | t0003 | g0077 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00609 | hp1 | a0001 | c0003 | t0003 | g0040 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00609 | hp2 | a0002 | c0004 | t0002 | g0054 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00673 | hp2 | a0002 | c0004 | t0002 | g0135 | EAS | CHS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0283 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00741 | hp1 | a0001 | c0010 | t0007 | g0059 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG00741 | hp2 | a0003 | c0007 | t0002 | g0201 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01069 | hp2 | a0001 | c0003 | t0004 | g0030 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01070 | hp1 | a0003 | c0007 | t0002 | g0245 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01071 | hp1 | a0003 | c0007 | t0002 | g0207 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01071 | hp2 | a0001 | c0003 | t0004 | g0030 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0286 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01167 | hp1 | a0001 | c0006 | t0006 | g0027 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01168 | hp1 | a0001 | c0003 | t0004 | g0173 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01169 | hp2 | a0001 | c0006 | t0006 | g0027 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0280 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01243 | hp1 | a0009 | c0024 | t0018 | g0175 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01255 | hp1 | a0003 | c0007 | t0002 | g0231 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01261 | hp1 | a0004 | c0009 | t0003 | g0008 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0138 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01433 | hp2 | a0003 | c0007 | t0002 | g0038 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01496 | hp1 | a0001 | c0011 | t0003 | g0072 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0124 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0229 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01516 | hp2 | a0003 | c0007 | t0002 | g0232 | EUR | IBS | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01884 | hp1 | a0001 | c0003 | t0004 | g0210 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01884 | hp2 | a0001 | c0006 | t0021 | g0182 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01891 | hp2 | a0001 | c0005 | t0001 | g0146 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01975 | hp2 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01978 | hp2 | a0003 | c0007 | t0002 | g0038 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG01993 | hp2 | a0001 | c0011 | t0003 | g0226 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02015 | hp1 | a0001 | c0003 | t0003 | g0268 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02015 | hp2 | a0001 | c0008 | t0002 | g0064 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02027 | hp2 | a0001 | c0003 | t0003 | g0265 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0269 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02055 | hp1 | a0001 | c0006 | t0005 | g0253 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02055 | hp2 | a0013 | c0026 | t0005 | g0174 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02056 | hp2 | a0002 | c0004 | t0002 | g0055 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02074 | hp1 | a0001 | c0003 | t0004 | g0152 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02080 | hp1 | a0001 | c0008 | t0002 | g0083 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02083 | hp2 | a0002 | c0004 | t0002 | g0071 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02129 | hp1 | a0002 | c0004 | t0002 | g0023 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0267 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02135 | hp2 | a0001 | c0008 | t0002 | g0112 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0190 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02155 | hp2 | a0002 | c0004 | t0002 | g0224 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02165 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | CDX | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02257 | hp1 | a0005 | c0012 | t0013 | g0252 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02257 | hp2 | a0001 | c0003 | t0004 | g0216 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0284 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02273 | hp2 | a0001 | c0011 | t0003 | g0073 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02451 | hp1 | a0001 | c0006 | t0006 | g0180 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02451 | hp2 | a0001 | c0003 | t0004 | g0176 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02523 | hp2 | a0001 | c0003 | t0003 | g0040 | EAS | KHV | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02572 | hp1 | a0001 | c0010 | t0007 | g0277 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02572 | hp2 | a0001 | c0003 | t0004 | g0250 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0187 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02615 | hp2 | a0001 | c0010 | t0007 | g0285 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02622 | hp1 | a0001 | c0003 | t0004 | g0191 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02622 | hp2 | a0001 | c0005 | t0001 | g0169 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0233 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02630 | hp2 | a0001 | c0003 | t0003 | g0193 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02647 | hp1 | a0001 | c0006 | t0017 | g0163 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02647 | hp2 | a0001 | c0006 | t0020 | g0081 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0004 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02723 | hp2 | a0001 | c0003 | t0004 | g0025 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02735 | hp2 | a0001 | c0003 | t0004 | g0031 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02809 | hp1 | a0001 | c0005 | t0001 | g0212 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02809 | hp2 | a0001 | c0014 | t0001 | g0214 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02818 | hp1 | a0001 | c0003 | t0016 | g0166 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02886 | hp1 | a0001 | c0006 | t0005 | g0256 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0171 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0035 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02896 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02897 | hp1 | a0001 | c0003 | t0004 | g0035 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02897 | hp2 | a0001 | c0005 | t0001 | g0183 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02922 | hp1 | a0006 | c0013 | t0022 | g0263 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02922 | hp2 | a0007 | c0015 | t0011 | g0261 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0213 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02970 | hp1 | a0001 | c0005 | t0001 | g0167 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02970 | hp2 | a0001 | c0003 | t0015 | g0161 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02976 | hp1 | a0005 | c0012 | t0013 | g0255 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02976 | hp2 | a0001 | c0003 | t0004 | g0211 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03017 | hp1 | a0002 | c0016 | t0010 | g0011 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0149 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03041 | hp2 | a0001 | c0003 | t0004 | g0025 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03098 | hp1 | a0001 | c0006 | t0005 | g0039 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0184 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03130 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03130 | hp2 | a0001 | c0003 | t0008 | g0254 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03139 | hp1 | a0001 | c0006 | t0005 | g0259 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03139 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03195 | hp1 | a0001 | c0010 | t0007 | g0287 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03195 | hp2 | a0001 | c0014 | t0001 | g0228 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03209 | hp1 | a0006 | c0013 | t0012 | g0029 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03209 | hp2 | a0001 | c0003 | t0003 | g0281 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03225 | hp1 | a0006 | c0013 | t0012 | g0029 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03453 | hp1 | a0001 | c0003 | t0003 | g0185 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03453 | hp2 | a0001 | c0006 | t0006 | g0170 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03486 | hp1 | a0001 | c0003 | t0004 | g0242 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03486 | hp2 | a0001 | c0003 | t0004 | g0209 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03516 | hp1 | a0001 | c0005 | t0001 | g0194 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03516 | hp2 | a0001 | c0003 | t0003 | g0032 | AFR | ESN | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03540 | hp1 | a0001 | c0010 | t0007 | g0282 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0107 | AFR | GWD | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03579 | hp1 | a0001 | c0006 | t0006 | g0251 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0247 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03669 | hp1 | a0011 | c0018 | t0001 | g0158 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0042 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0041 | SAS | PJL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03831 | hp1 | a0002 | c0004 | t0002 | g0046 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03927 | hp1 | a0001 | c0003 | t0004 | g0177 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03942 | hp1 | a0002 | c0002 | t0014 | g0099 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03942 | hp2 | a0002 | c0027 | t0002 | g0087 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG04115 | hp1 | a0002 | c0016 | t0010 | g0011 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG04184 | hp1 | a0001 | c0003 | t0004 | g0159 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0104 | SAS | BEB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0100 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG04228 | hp2 | a0001 | c0003 | t0004 | g0116 | SAS | STU | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18522 | hp1 | a0001 | c0006 | t0005 | g0260 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0153 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18612 | hp1 | a0002 | c0004 | t0002 | g0012 | EAS | CHB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18612 | hp2 | a0002 | c0004 | t0002 | g0036 | EAS | CHB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18906 | hp1 | a0001 | c0023 | t0004 | g0168 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0188 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18941 | hp1 | a0002 | c0004 | t0002 | g0078 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18946 | hp1 | a0001 | c0008 | t0002 | g0074 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18951 | hp2 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18957 | hp2 | a0002 | c0004 | t0002 | g0276 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18960 | hp2 | a0004 | c0009 | t0003 | g0050 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18961 | hp2 | a0001 | c0003 | t0004 | g0097 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18967 | hp1 | a0001 | c0001 | t0009 | g0248 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18967 | hp2 | a0001 | c0003 | t0003 | g0142 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18968 | hp2 | a0004 | c0009 | t0003 | g0008 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18969 | hp1 | a0001 | c0003 | t0003 | g0126 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18971 | hp1 | a0001 | c0003 | t0003 | g0106 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18972 | hp1 | a0008 | c0022 | t0004 | g0147 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18973 | hp2 | a0002 | c0004 | t0002 | g0279 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18974 | hp1 | a0002 | c0004 | t0002 | g0023 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18977 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18978 | hp2 | a0001 | c0003 | t0004 | g0155 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18985 | hp1 | a0002 | c0004 | t0002 | g0037 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18985 | hp2 | a0001 | c0003 | t0004 | g0151 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18995 | hp1 | a0002 | c0004 | t0002 | g0202 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18995 | hp2 | a0001 | c0008 | t0002 | g0088 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18998 | hp1 | a0001 | c0003 | t0003 | g0090 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18999 | hp1 | a0001 | c0008 | t0002 | g0084 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA18999 | hp2 | a0001 | c0003 | t0003 | g0274 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19000 | hp1 | a0001 | c0003 | t0004 | g0150 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19000 | hp2 | a0002 | c0004 | t0002 | g0016 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0218 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0272 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19011 | hp1 | a0002 | c0004 | t0002 | g0037 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19012 | hp1 | a0004 | c0009 | t0003 | g0008 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19030 | hp1 | a0001 | c0003 | t0003 | g0246 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19030 | hp2 | a0001 | c0006 | t0005 | g0039 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0186 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19043 | hp2 | a0001 | c0025 | t0001 | g0262 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19054 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19058 | hp2 | a0001 | c0003 | t0004 | g0026 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19060 | hp1 | a0002 | c0004 | t0002 | g0076 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19062 | hp2 | a0001 | c0003 | t0003 | g0266 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19064 | hp2 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19067 | hp2 | a0001 | c0003 | t0004 | g0148 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19070 | hp1 | a0001 | c0003 | t0003 | g0117 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19074 | hp1 | a0002 | c0004 | t0002 | g0036 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19074 | hp2 | a0004 | c0009 | t0003 | g0093 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19079 | hp2 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19083 | hp2 | a0004 | c0009 | t0003 | g0086 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19085 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19085 | hp2 | a0002 | c0004 | t0002 | g0236 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19088 | hp1 | a0001 | c0003 | t0004 | g0160 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19088 | hp2 | a0002 | c0004 | t0002 | g0012 | EAS | JPT | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19240 | hp1 | a0001 | c0003 | t0008 | g0257 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | YRI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20129 | hp2 | a0005 | c0021 | t0019 | g0164 | AFR | ASW | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20752 | hp1 | a0014 | c0020 | t0001 | g0045 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20905 | hp2 | a0002 | c0002 | t0014 | g0091 | SAS | GIH | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02109 | hp1 | a0001 | c0003 | t0008 | g0258 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02559 | hp1 | a0001 | c0006 | t0006 | g0179 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG03471 | hp2 | a0007 | c0015 | t0011 | g0264 | AFR | MSL | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG06807 | hp1 | a0001 | c0003 | t0003 | g0004 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
HG06807 | hp2 | a0001 | c0003 | t0004 | g0068 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20300 | hp1 | a0010 | c0017 | t0001 | g0028 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0048 | AFR | USA | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA21309 | hp1 | a0005 | c0012 | t0006 | g0133 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0215 | AFR | LWK | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0002 | REF | REF | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | DSG2_chr18_31493177_31554008 | DSG2 | chr18 | 31493177 | 31554008 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31524751
|
A | G | 1 | a0014 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.877A>G | p.Ile293Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/15 | 952/5697 | 877/3357 | 293/1118 | chr18 | 31524751 | ||
chr18:31536321
|
G | A | 1 | a0005 | 4 | HG02257.hp1 HG02976.hp1 NA20129.hp2 others(1): Show |
missense_variant | MODERATE | c.1543G>A | p.Val515Ile | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/15 | 1618/5697 | 1543/3357 | 515/1118 | chr18 | 31536321 | ||
chr18:31536328
|
C | T | 1 | a0013 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1550C>T | p.Ala517Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/15 | 1625/5697 | 1550/3357 | 517/1118 | chr18 | 31536328 | ||
chr18:31536375
|
G | A | 1 | a0008 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.1597G>A | p.Val533Ile | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/15 | 1672/5697 | 1597/3357 | 533/1118 | chr18 | 31536375 | ||
chr18:31542655
|
G | A | 1 | a0003 | 8 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(5): Show |
missense_variant | MODERATE | c.2137G>A | p.Glu713Lys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2212/5697 | 2137/3357 | 713/1118 | chr18 | 31542655 | ||
chr18:31542791
|
C | T | 1 | a0012 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.2273C>T | p.Ala758Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2348/5697 | 2273/3357 | 758/1118 | chr18 | 31542791 | ||
chr18:31542836
|
G | A | 2 | a0002a0003 | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
missense_variant | MODERATE | c.2318G>A | p.Arg773Lys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2393/5697 | 2318/3357 | 773/1118 | chr18 | 31542836 | ||
chr18:31545973
|
A | C | 1 | a0006 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.2587A>C | p.Met863Leu | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2662/5697 | 2587/3357 | 863/1118 | chr18 | 31545973 | ||
chr18:31546033
|
T | C | 2 | a0009a0010 | 2 | HG01243.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.2647T>C | p.Ser883Pro | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2722/5697 | 2647/3357 | 883/1118 | chr18 | 31546033 | ||
chr18:31546094
|
C | T | 1 | a0009 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2708C>T | p.Thr903Ile | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2783/5697 | 2708/3357 | 903/1118 | chr18 | 31546094 | ||
chr18:31546272
|
T | G | 1 | a0007 | 2 | HG02922.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.2886T>G | p.Ile962Met | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2961/5697 | 2886/3357 | 962/1118 | chr18 | 31546272 | ||
chr18:31546292
|
C | T | 1 | a0011 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.2906C>T | p.Ala969Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2981/5697 | 2906/3357 | 969/1118 | chr18 | 31546292 | ||
chr18:31546595
|
C | T | 1 | a0004 | 6 | HG01261.hp1 NA18960.hp2 NA18968.hp2 others(3): Show |
missense_variant | MODERATE | c.3209C>T | p.Thr1070Met | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3284/5697 | 3209/3357 | 1070/1118 | chr18 | 31546595 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31520859
|
A | G | 1 | a0002c0027 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.273A>G | p.Gly91Gly | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 4/15 | 348/5697 | 273/3357 | 91/1118 | chr18 | 31520859 | ||
chr18:31524735
|
C | T | 18 | a0001c0003a0001c0005a0001c0006others(15): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
synonymous_variant | LOW | c.861C>T | p.Asn287Asn | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/15 | 936/5697 | 861/3357 | 287/1118 | chr18 | 31524735 | ||
chr18:31538974
|
G | C | 1 | a0001c0023 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1875G>C | p.Leu625Leu | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/15 | 1950/5697 | 1875/3357 | 625/1118 | chr18 | 31538974 | ||
chr18:31541224
|
C | T | 1 | a0002c0016 | 2 | HG03017.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.1911C>T | p.Cys637Cys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/15 | 1986/5697 | 1911/3357 | 637/1118 | chr18 | 31541224 | ||
chr18:31541227
|
A | G | 1 | a0002c0016 | 2 | HG03017.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.1914A>G | p.Gly638Gly | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/15 | 1989/5697 | 1914/3357 | 638/1118 | chr18 | 31541227 | ||
chr18:31542729
|
C | T | 1 | a0007c0015 | 2 | HG02922.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2211C>T | p.Gly737Gly | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/15 | 2286/5697 | 2211/3357 | 737/1118 | chr18 | 31542729 | ||
chr18:31545870
|
T | C | 1 | a0013c0026 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2484T>C | p.Asp828Asp | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2559/5697 | 2484/3357 | 828/1118 | chr18 | 31545870 | ||
chr18:31545891
|
A | G | 6 | a0001c0003a0001c0011a0001c0023others(3): Show | 85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
synonymous_variant | LOW | c.2505A>G | p.Thr835Thr | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2580/5697 | 2505/3357 | 835/1118 | chr18 | 31545891 | ||
chr18:31545972
|
T | C | 1 | a0007c0015 | 2 | HG02922.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2586T>C | p.Ser862Ser | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2661/5697 | 2586/3357 | 862/1118 | chr18 | 31545972 | ||
chr18:31546089
|
A | G | 1 | a0001c0025 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2703A>G | p.Lys901Lys | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2778/5697 | 2703/3357 | 901/1118 | chr18 | 31546089 | ||
chr18:31546521
|
A | C | 1 | a0001c0014 | 2 | HG02809.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.3135A>C | p.Thr1045Thr | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3210/5697 | 3135/3357 | 1045/1118 | chr18 | 31546521 | ||
chr18:31546629
|
C | T | 1 | a0001c0010 | 5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
synonymous_variant | LOW | c.3243C>T | p.Val1081Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3318/5697 | 3243/3357 | 1081/1118 | chr18 | 31546629 | ||
chr18:31546707
|
T | C | 19 | a0001c0003a0001c0006a0001c0008others(16): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
synonymous_variant | LOW | c.3321T>C | p.Val1107Val | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3396/5697 | 3321/3357 | 1107/1118 | chr18 | 31546707 | ||
chr18:31546719
|
C | T | 1 | a0005c0021 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3333C>T | p.Ser1111Ser | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 3408/5697 | 3333/3357 | 1111/1118 | chr18 | 31546719 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31546874
|
C | T | 1 | a0006c0013t0022 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 131 | chr18 | 31546874 | |||||
chr18:31546981
|
T | G | 1 | a0002c0016t0010 | 2 | HG03017.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*238T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 238 | chr18 | 31546981 | |||||
chr18:31547190
|
A | G | 1 | a0001c0006t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 447 | chr18 | 31547190 | |||||
chr18:31547308
|
A | G | 6 | a0001c0008t0002a0002c0002t0002a0002c0002t0014others(3): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*565A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 565 | chr18 | 31547308 | |||||
chr18:31547341
|
CAG | C | 1 | a0001c0001t0009 | 3 | NA18944.hp1 NA18967.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599_*600delAG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 599 | chr18 | 31547341 | |||||
chr18:31547342
|
A | AGT | 5 | a0001c0003t0004a0001c0006t0020a0001c0010t0007others(2): Show | 42 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*611_*612dupTG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 613 | INFO_REALIGN_3_PRIME | chr18 | 31547342 | ||||
chr18:31547420
|
T | C | 1 | a0001c0003t0008 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*677T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 677 | chr18 | 31547420 | |||||
chr18:31547448
|
G | A | 1 | a0007c0015t0011 | 2 | HG02922.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*705G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 705 | chr18 | 31547448 | |||||
chr18:31547550
|
G | A | 1 | a0007c0015t0011 | 2 | HG02922.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 807 | chr18 | 31547550 | |||||
chr18:31547676
|
C | CA | 11 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(8): Show | 89 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*944dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 945 | INFO_REALIGN_3_PRIME | chr18 | 31547676 | ||||
chr18:31547694
|
G | GA | 2 | a0001c0006t0005a0013c0026t0005 | 7 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*960dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 961 | INFO_REALIGN_3_PRIME | chr18 | 31547694 | ||||
chr18:31547732
|
C | T | 1 | a0001c0006t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*989C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 989 | chr18 | 31547732 | |||||
chr18:31547779
|
C | G | 1 | a0001c0006t0020 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1036C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1036 | chr18 | 31547779 | |||||
chr18:31547794
|
T | C | 1 | a0001c0006t0017 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1051T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1051 | chr18 | 31547794 | |||||
chr18:31547814
|
T | C | 1 | a0002c0002t0014 | 2 | HG03942.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1071T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1071 | chr18 | 31547814 | |||||
chr18:31548007
|
G | A | 1 | a0009c0024t0018 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1264 | chr18 | 31548007 | |||||
chr18:31548007
|
G | C | 1 | a0001c0003t0015 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1264 | chr18 | 31548007 | |||||
chr18:31548082
|
G | A | 8 | a0001c0003t0004a0001c0003t0016a0001c0006t0020others(5): Show | 46 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1339G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1339 | chr18 | 31548082 | |||||
chr18:31548128
|
C | T | 2 | a0001c0006t0021a0005c0012t0013 | 3 | HG01884.hp2 HG02257.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1385C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1385 | chr18 | 31548128 | |||||
chr18:31548132
|
A | T | 1 | a0001c0006t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1389A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1389 | chr18 | 31548132 | |||||
chr18:31548214
|
T | C | 1 | a0002c0016t0010 | 2 | HG03017.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1471T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1471 | chr18 | 31548214 | |||||
chr18:31548417
|
G | A | 1 | a0005c0021t0019 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1674G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1674 | chr18 | 31548417 | |||||
chr18:31548455
|
C | CTG | 29 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(26): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1714_*1715dupGT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1716 | INFO_REALIGN_3_PRIME | chr18 | 31548455 | ||||
chr18:31548587
|
A | G | 2 | a0006c0013t0012a0006c0013t0022 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1844A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1844 | chr18 | 31548587 | |||||
chr18:31548609
|
T | C | 30 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(27): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1866T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1866 | chr18 | 31548609 | |||||
chr18:31548703
|
C | T | 1 | a0007c0015t0011 | 2 | HG02922.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1960C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 1960 | chr18 | 31548703 | |||||
chr18:31548905
|
CAGTT | C | 14 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(11): Show | 95 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2163_*2166delAGTT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2163 | chr18 | 31548905 | |||||
chr18:31548916
|
G | A | 14 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(11): Show | 95 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2173G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2173 | chr18 | 31548916 | |||||
chr18:31548988
|
G | A | 30 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(27): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2245G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 15/15 | 2245 | chr18 | 31548988 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31498370
|
C | G | 8 | a0001c0003t0003g0281a0001c0005t0001g0284a0001c0010t0007g0282others(5): Show | 8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+74C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498370 | ||||||
chr18:31498443
|
C | T | 1 | a0002c0004t0002g0279 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.45+147C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498443 | ||||||
chr18:31498471
|
G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+175G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498471 | ||||||
chr18:31498488
|
C | T | 1 | a0002c0002t0002g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.45+192C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498488 | ||||||
chr18:31498553
|
A | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(109): Show | 136 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.45+257A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498553 | ||||||
chr18:31498652
|
C | G | 7 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(4): Show | 10 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+356C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498652 | ||||||
chr18:31498664
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(163): Show | 200 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.45+368A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498664 | ||||||
chr18:31498817
|
A | T | 1 | a0001c0006t0021g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+521A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498817 | ||||||
chr18:31498841
|
A | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0006t0006g0179others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+545A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498841 | ||||||
chr18:31498859
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0006t0006g0179others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+563C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31498859 | ||||||
chr18:31499001
|
C | T | 2 | a0001c0003t0004g0031a0001c0003t0004g0177 | 3 | HG00140.hp2 HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.45+705C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499001 | ||||||
chr18:31499093
|
G | T | 8 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(5): Show | 11 | HG02572.hp1 HG02615.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+797G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499093 | ||||||
chr18:31499203
|
C | A | 1 | a0002c0002t0002g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.45+907C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499203 | ||||||
chr18:31499205
|
C | T | 15 | a0001c0001t0001g0273a0001c0003t0003g0004a0001c0003t0003g0040others(12): Show | 20 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+909C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499205 | ||||||
chr18:31499237
|
T | G | 36 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(33): Show | 43 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.45+941T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499237 | ||||||
chr18:31499272
|
C | G | 4 | a0001c0001t0001g0162a0001c0006t0006g0027a0001c0006t0017g0163others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+976C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499272 | ||||||
chr18:31499306
|
C | T | 4 | a0001c0001t0001g0162a0001c0006t0006g0027a0001c0006t0017g0163others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1010C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499306 | ||||||
chr18:31499357
|
C | CGT | 83 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0089others(80): Show | 104 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.45+1090_45+1091dup others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | |||||
chr18:31499357
|
C | CGTGT | 8 | a0001c0001t0001g0143a0001c0003t0003g0141a0001c0003t0003g0142others(5): Show | 9 | HG00140.hp2 HG01884.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+1088_45+1091dup others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | |||||
chr18:31499357
|
C | CGTGTGT | 3 | a0001c0003t0004g0176a0002c0002t0002g0144a0009c0024t0018g0175 | 3 | HG01243.hp1 HG02080.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.45+1086_45+1091dup others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | |||||
chr18:31499357
|
CGT | C | 3 | a0001c0003t0004g0250a0001c0003t0015g0161a0014c0020t0001g0045 | 3 | HG02572.hp2 HG02970.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.45+1090_45+1091del others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | |||||
chr18:31499357
|
CGTGT | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 156 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.45+1088_45+1091del others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | |||||
chr18:31499357
|
CGTGTGTG others(3): Show |
C | 1 | a0002c0002t0002g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.45+1082_45+1091del others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31499357 | |||||
chr18:31499369
|
T | C | 2 | a0001c0003t0004g0250a0001c0003t0015g0161 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.45+1073T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499369 | ||||||
chr18:31499371
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(121): Show | 154 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.45+1075T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499371 | ||||||
chr18:31499639
|
C | T | 9 | a0001c0003t0003g0281a0001c0005t0001g0284a0001c0010t0007g0282others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+1343C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499639 | ||||||
chr18:31499641
|
T | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+1345T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499641 | ||||||
chr18:31499649
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.45+1353T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31499649 | ||||||
chr18:31500036
|
T | TA | 43 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0089others(40): Show | 45 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.45+1763dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | |||||
chr18:31500036
|
T | TAA | 11 | a0001c0001t0001g0178a0001c0003t0008g0254a0001c0006t0005g0039others(8): Show | 13 | HG01070.hp1 HG01175.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+1762_45+1763dup others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | |||||
chr18:31500036
|
T | TAAA | 67 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(64): Show | 86 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.45+1761_45+1763dup others(3): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | |||||
chr18:31500036
|
T | TAAAA | 20 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0197others(17): Show | 24 | HG00741.hp2 HG01069.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.45+1760_45+1763dup others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31500036 | |||||
chr18:31500066
|
G | A | 1 | a0001c0003t0016g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+1770G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500066 | ||||||
chr18:31500122
|
A | C | 1 | a0001c0008t0002g0084 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.45+1826A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500122 | ||||||
chr18:31500132
|
G | C | 1 | a0001c0008t0002g0084 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.45+1836G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500132 | ||||||
chr18:31500170
|
T | G | 2 | a0001c0001t0001g0092a0002c0002t0002g0017 | 3 | HG00323.hp2 HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.45+1874T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500170 | ||||||
chr18:31500206
|
G | A | 4 | a0001c0001t0001g0162a0001c0006t0006g0027a0001c0006t0017g0163others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1910G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500206 | ||||||
chr18:31500596
|
A | T | 4 | a0001c0001t0001g0162a0001c0006t0006g0027a0001c0006t0017g0163others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+2300A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500596 | ||||||
chr18:31500684
|
G | A | 39 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(36): Show | 46 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+2388G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500684 | ||||||
chr18:31500793
|
A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+2497A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31500793 | ||||||
chr18:31501112
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(149): Show | 183 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.45+2816C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501112 | ||||||
chr18:31501241
|
C | T | 1 | a0006c0013t0022g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+2945C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501241 | ||||||
chr18:31501497
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+3201C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501497 | ||||||
chr18:31501685
|
G | C | 4 | a0001c0003t0003g0032a0001c0003t0003g0190a0001c0003t0003g0246others(1): Show | 5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3389G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501685 | ||||||
chr18:31501797
|
C | G | 39 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(36): Show | 46 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+3501C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501797 | ||||||
chr18:31501865
|
T | A | 5 | a0002c0002t0002g0094a0004c0009t0003g0008a0004c0009t0003g0050others(2): Show | 7 | HG01261.hp1 HG02040.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+3569T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501865 | ||||||
chr18:31501966
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+3670G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31501966 | ||||||
chr18:31502149
|
T | G | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+3853T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502149 | ||||||
chr18:31502229
|
T | G | 1 | a0002c0002t0002g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.45+3933T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502229 | ||||||
chr18:31502268
|
T | C | 36 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(33): Show | 44 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.45+3972T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502268 | ||||||
chr18:31502409
|
T | C | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+4113T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502409 | ||||||
chr18:31502531
|
C | G | 3 | a0001c0003t0008g0254a0005c0012t0013g0252a0005c0012t0013g0255 | 3 | HG02257.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45+4235C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502531 | ||||||
chr18:31502675
|
TGGAAGGC others(3): Show |
T | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+4382_45+4391del others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31502675 | |||||
chr18:31502736
|
G | A | 1 | a0002c0002t0002g0096 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.45+4440G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502736 | ||||||
chr18:31502888
|
G | T | 1 | a0001c0001t0001g0007 | 4 | NA18963.hp1 NA18968.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+4592G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502888 | ||||||
chr18:31502996
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 199 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.45+4700G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31502996 | ||||||
chr18:31503051
|
C | T | 1 | a0001c0006t0006g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.45+4755C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503051 | ||||||
chr18:31503053
|
G | A | 40 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(37): Show | 48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+4757G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503053 | ||||||
chr18:31503298
|
G | A | 1 | a0001c0005t0001g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+5002G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503298 | ||||||
chr18:31503303
|
A | G | 8 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(5): Show | 11 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+5007A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503303 | ||||||
chr18:31503377
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0243 | 4 | HG00423.hp2 HG02083.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5081A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503377 | ||||||
chr18:31503402
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.45+5106G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503402 | ||||||
chr18:31503427
|
G | C | 1 | a0001c0010t0007g0277 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.45+5131G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503427 | ||||||
chr18:31503460
|
T | C | 1 | a0002c0004t0002g0046 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.45+5164T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503460 | ||||||
chr18:31503599
|
G | A | 40 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(37): Show | 48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+5303G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503599 | ||||||
chr18:31503657
|
A | G | 1 | a0001c0010t0007g0287 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+5361A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503657 | ||||||
chr18:31503667
|
G | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(125): Show | 154 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.45+5371G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503667 | ||||||
chr18:31503668
|
C | T | 4 | a0001c0003t0003g0032a0001c0003t0003g0190a0001c0003t0003g0246others(1): Show | 5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+5372C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503668 | ||||||
chr18:31503820
|
G | A | 8 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(5): Show | 11 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+5524G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503820 | ||||||
chr18:31503925
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 199 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.45+5629G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503925 | ||||||
chr18:31503979
|
G | T | 8 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(5): Show | 11 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+5683G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31503979 | ||||||
chr18:31504142
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.45+5846G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504142 | ||||||
chr18:31504458
|
T | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(150): Show | 185 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.45+6162T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504458 | ||||||
chr18:31504553
|
T | TG | 40 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(37): Show | 48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+6260dupG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31504553 | |||||
chr18:31504718
|
C | T | 4 | a0001c0001t0001g0162a0001c0006t0006g0027a0001c0006t0017g0163others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+6422C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504718 | ||||||
chr18:31504878
|
C | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+6582C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504878 | ||||||
chr18:31504925
|
A | G | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+6629A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504925 | ||||||
chr18:31504986
|
C | T | 1 | a0001c0003t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+6690C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31504986 | ||||||
chr18:31505003
|
T | G | 1 | a0001c0003t0004g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.45+6707T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505003 | ||||||
chr18:31505110
|
A | G | 1 | a0002c0002t0002g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.45+6814A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505110 | ||||||
chr18:31505336
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.45+7040C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505336 | ||||||
chr18:31505527
|
G | A | 1 | a0002c0002t0002g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.45+7231G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505527 | ||||||
chr18:31505555
|
A | G | 2 | a0001c0006t0006g0170a0013c0026t0005g0174 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.45+7259A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505555 | ||||||
chr18:31505656
|
C | CT | 45 | a0001c0001t0001g0049a0001c0001t0001g0082a0001c0001t0001g0137others(42): Show | 52 | HG00673.hp2 HG01106.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+7375dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31505656 | |||||
chr18:31505656
|
CT | C | 24 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0162others(21): Show | 28 | HG00140.hp2 HG00609.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+7375delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31505656 | |||||
chr18:31505786
|
C | T | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+7490C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505786 | ||||||
chr18:31505815
|
C | G | 33 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(30): Show | 40 | HG01891.hp2 HG02074.hp1 HG02165.hp2 others(37): Show |
intron_variant | MODIFIER | c.45+7519C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505815 | ||||||
chr18:31505863
|
T | C | 1 | a0001c0005t0001g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.45+7567T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505863 | ||||||
chr18:31505899
|
C | T | 3 | a0001c0003t0004g0025a0002c0002t0002g0149a0006c0013t0012g0029 | 5 | HG02723.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+7603C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31505899 | ||||||
chr18:31506085
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(151): Show | 186 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+7789A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506085 | ||||||
chr18:31506229
|
G | A | 3 | a0001c0003t0008g0254a0005c0012t0013g0252a0005c0012t0013g0255 | 3 | HG02257.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45+7933G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506229 | ||||||
chr18:31506376
|
T | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.45+8080T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506376 | ||||||
chr18:31506413
|
C | T | 1 | a0001c0003t0003g0080 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.45+8117C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506413 | ||||||
chr18:31506486
|
A | G | 40 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(37): Show | 48 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.45+8190A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506486 | ||||||
chr18:31506669
|
AGT | A | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8375_45+8376del others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31506669 | |||||
chr18:31506678
|
A | G | 1 | a0001c0003t0003g0274 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.45+8382A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506678 | ||||||
chr18:31506689
|
T | G | 12 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0003t0003g0185others(9): Show | 15 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+8393T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506689 | ||||||
chr18:31506884
|
C | T | 2 | a0001c0006t0006g0170a0013c0026t0005g0174 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.45+8588C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506884 | ||||||
chr18:31506893
|
G | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 201 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.45+8597G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31506893 | ||||||
chr18:31507010
|
T | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(284): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.45+8714T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507010 | ||||||
chr18:31507037
|
C | G | 2 | a0001c0005t0001g0167a0001c0023t0004g0168 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8741C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507037 | ||||||
chr18:31507138
|
C | T | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+8842C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507138 | ||||||
chr18:31507149
|
TC | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(284): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.45+8857delC | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31507149 | |||||
chr18:31507198
|
T | G | 24 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(21): Show | 28 | HG01891.hp2 HG02074.hp1 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+8902T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507198 | ||||||
chr18:31507689
|
C | A | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+9393C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507689 | ||||||
chr18:31507789
|
T | C | 2 | a0002c0002t0002g0100a0002c0002t0014g0099 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.45+9493T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31507789 | ||||||
chr18:31508010
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(151): Show | 186 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+9714A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508010 | ||||||
chr18:31508015
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0006t0006g0179others(1): Show | 4 | HG02451.hp1 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9719G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508015 | ||||||
chr18:31508100
|
T | G | 1 | a0001c0006t0020g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+9804T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508100 | ||||||
chr18:31508145
|
G | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0143 | 3 | HG01243.hp2 HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.45+9849G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508145 | ||||||
chr18:31508185
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(151): Show | 186 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+9889G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508185 | ||||||
chr18:31508231
|
G | A | 2 | a0001c0005t0001g0145a0001c0005t0001g0146 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.45+9935G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508231 | ||||||
chr18:31508289
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.46-9950T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508289 | ||||||
chr18:31508353
|
A | ATTTAT | 15 | a0001c0001t0001g0165a0001c0001t0001g0189a0001c0001t0001g0234others(12): Show | 16 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-9838_46-9834dup others(5): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508353
|
A | ATTTATTT others(3): Show |
1 | a0001c0003t0003g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-9843_46-9834dup others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508353
|
A | ATTTATTT others(8): Show |
1 | a0001c0001t0001g0238 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-9848_46-9834dup others(15): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508353
|
ATTTAT | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0043others(21): Show | 27 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.46-9838_46-9834del others(5): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508353
|
ATTTATTT others(3): Show |
A | 60 | a0001c0001t0001g0102a0001c0001t0001g0154a0001c0001t0001g0156others(57): Show | 71 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.46-9843_46-9834del others(10): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508353
|
ATTTATTT others(8): Show |
A | 8 | a0001c0001t0001g0052a0001c0001t0001g0162a0001c0003t0016g0166others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9848_46-9834del others(15): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508353
|
ATTTATTT others(18): Show |
A | 12 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0003t0003g0185others(9): Show | 15 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-9858_46-9834del others(25): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31508353 | |||||
chr18:31508429
|
C | T | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.46-9810C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508429 | ||||||
chr18:31508463
|
G | A | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.46-9776G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508463 | ||||||
chr18:31508746
|
G | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(163): Show | 200 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.46-9493G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508746 | ||||||
chr18:31508913
|
T | G | 2 | a0001c0001t0009g0033a0001c0001t0009g0248 | 3 | NA18944.hp1 NA18967.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.46-9326T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508913 | ||||||
chr18:31508995
|
C | T | 37 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(34): Show | 45 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.46-9244C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31508995 | ||||||
chr18:31509056
|
AAAG | A | 9 | a0001c0003t0003g0281a0001c0005t0001g0284a0001c0010t0007g0282others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-9178_46-9176del others(3): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31509056 | |||||
chr18:31509246
|
T | C | 1 | a0001c0003t0016g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-8993T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509246 | ||||||
chr18:31509264
|
A | G | 5 | a0002c0002t0002g0024a0002c0002t0002g0129a0002c0002t0002g0130others(2): Show | 6 | HG01928.hp1 HG01943.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8975A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509264 | ||||||
chr18:31509389
|
G | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0208a0002c0002t0002g0034others(1): Show | 5 | HG02148.hp2 NA18946.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8850G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509389 | ||||||
chr18:31509402
|
G | A | 8 | a0001c0003t0008g0257a0001c0003t0008g0258a0001c0006t0005g0039others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-8837G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509402 | ||||||
chr18:31509421
|
A | G | 1 | a0007c0015t0011g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-8818A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509421 | ||||||
chr18:31509432
|
C | CT | 131 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(128): Show | 166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.46-8798dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31509432 | |||||
chr18:31509432
|
C | CTT | 155 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(152): Show | 186 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.46-8799_46-8798dup others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31509432 | |||||
chr18:31509598
|
T | C | 4 | a0001c0003t0008g0254a0001c0006t0006g0251a0005c0012t0013g0252others(1): Show | 4 | HG02257.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8641T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509598 | ||||||
chr18:31509922
|
T | A | 12 | a0001c0001t0001g0172a0001c0003t0004g0030a0001c0003t0004g0031others(9): Show | 14 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.46-8317T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509922 | ||||||
chr18:31509975
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.46-8264G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31509975 | ||||||
chr18:31510175
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.46-8064G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510175 | ||||||
chr18:31510226
|
C | T | 8 | a0001c0005t0001g0284a0001c0010t0007g0282a0001c0010t0007g0285others(5): Show | 8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-8013C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510226 | ||||||
chr18:31510227
|
G | A | 1 | a0001c0003t0004g0057 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.46-8012G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510227 | ||||||
chr18:31510259
|
T | G | 4 | a0001c0003t0008g0254a0001c0006t0006g0251a0005c0012t0013g0252others(1): Show | 4 | HG02257.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-7980T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510259 | ||||||
chr18:31510513
|
C | A | 1 | a0001c0003t0004g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-7726C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510513 | ||||||
chr18:31510590
|
G | GA | 4 | a0001c0005t0001g0006a0001c0005t0001g0183a0001c0025t0001g0262others(1): Show | 7 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-7636dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31510590 | |||||
chr18:31510606
|
T | C | 3 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0023t0004g0168 | 3 | HG02818.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.46-7633T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510606 | ||||||
chr18:31510671
|
T | G | 6 | a0001c0003t0003g0193a0001c0003t0004g0035a0001c0003t0004g0191others(3): Show | 7 | HG01884.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-7568T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510671 | ||||||
chr18:31510711
|
C | A | 12 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0003t0003g0185others(9): Show | 15 | HG02451.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-7528C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510711 | ||||||
chr18:31510771
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(124): Show | 153 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.46-7468A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510771 | ||||||
chr18:31510854
|
C | T | 1 | a0002c0002t0002g0127 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.46-7385C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510854 | ||||||
chr18:31510930
|
C | T | 15 | a0001c0001t0001g0162a0001c0001t0001g0178a0001c0001t0001g0181others(12): Show | 19 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-7309C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510930 | ||||||
chr18:31510954
|
A | G | 2 | a0001c0010t0007g0277a0007c0015t0011g0261 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.46-7285A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31510954 | ||||||
chr18:31511060
|
G | T | 4 | a0001c0003t0004g0153a0001c0003t0015g0161a0002c0002t0002g0149others(1): Show | 5 | HG02970.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-7179G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511060 | ||||||
chr18:31511068
|
A | G | 16 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(13): Show | 17 | HG01891.hp2 HG02074.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.46-7171A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511068 | ||||||
chr18:31511322
|
G | T | 1 | a0001c0001t0001g0238 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-6917G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511322 | ||||||
chr18:31511400
|
G | A | 1 | a0007c0015t0011g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-6839G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511400 | ||||||
chr18:31511412
|
C | T | 12 | a0001c0008t0002g0074a0001c0011t0003g0072a0001c0011t0003g0073others(9): Show | 14 | HG00438.hp1 HG00597.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-6827C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511412 | ||||||
chr18:31511551
|
A | T | 1 | a0002c0004t0002g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-6688A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511551 | ||||||
chr18:31511620
|
A | G | 1 | a0001c0003t0004g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.46-6619A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511620 | ||||||
chr18:31511938
|
G | A | 64 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0157others(61): Show | 73 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.46-6301G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31511938 | ||||||
chr18:31512053
|
G | A | 2 | a0001c0003t0003g0215a0001c0014t0001g0214 | 2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.46-6186G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512053 | ||||||
chr18:31512080
|
C | T | 1 | a0001c0003t0003g0272 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46-6159C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512080 | ||||||
chr18:31512326
|
A | G | 1 | a0001c0003t0015g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.46-5913A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512326 | ||||||
chr18:31512447
|
G | A | 3 | a0001c0003t0004g0025a0002c0002t0002g0149a0006c0013t0012g0029 | 5 | HG02723.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-5792G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512447 | ||||||
chr18:31512452
|
A | G | 1 | a0005c0012t0006g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-5787A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512452 | ||||||
chr18:31512656
|
A | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(157): Show | 194 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.46-5583A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512656 | ||||||
chr18:31512661
|
T | C | 1 | a0001c0005t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46-5578T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512661 | ||||||
chr18:31512798
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.46-5441T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512798 | ||||||
chr18:31512837
|
C | T | 1 | a0002c0004t0002g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.46-5402C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512837 | ||||||
chr18:31512881
|
A | G | 6 | a0001c0003t0004g0025a0001c0003t0004g0153a0001c0003t0015g0161others(3): Show | 8 | HG01884.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-5358A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31512881 | ||||||
chr18:31513129
|
C | A | 6 | a0001c0003t0004g0025a0001c0003t0004g0153a0001c0003t0015g0161others(3): Show | 8 | HG01884.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-5110C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513129 | ||||||
chr18:31513130
|
C | T | 4 | a0001c0005t0001g0169a0001c0006t0006g0170a0009c0024t0018g0175others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-5109C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513130 | ||||||
chr18:31513140
|
T | C | 1 | a0001c0006t0006g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-5099T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513140 | ||||||
chr18:31513181
|
A | G | 2 | a0002c0016t0010g0011a0005c0012t0006g0133 | 3 | HG03017.hp1 HG04115.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.46-5058A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513181 | ||||||
chr18:31513191
|
G | A | 1 | a0002c0002t0002g0139 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.46-5048G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513191 | ||||||
chr18:31513211
|
A | G | 1 | a0001c0006t0006g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-5028A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513211 | ||||||
chr18:31513354
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(156): Show | 193 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.46-4885A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513354 | ||||||
chr18:31513563
|
G | C | 1 | a0001c0003t0004g0177 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.46-4676G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513563 | ||||||
chr18:31513683
|
T | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(132): Show | 162 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.46-4556T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513683 | ||||||
chr18:31513698
|
C | T | 5 | a0001c0003t0016g0166a0001c0005t0001g0167a0001c0005t0001g0212others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-4541C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513698 | ||||||
chr18:31513908
|
A | T | 14 | a0001c0003t0004g0025a0001c0003t0004g0153a0001c0003t0008g0257others(11): Show | 17 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-4331A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31513908 | ||||||
chr18:31514071
|
T | C | 1 | a0002c0002t0002g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-4168T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514071 | ||||||
chr18:31514146
|
T | G | 10 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(7): Show | 14 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-4093T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514146 | ||||||
chr18:31514371
|
G | A | 9 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0005t0001g0006others(6): Show | 13 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-3868G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514371 | ||||||
chr18:31514388
|
T | C | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.46-3851T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514388 | ||||||
chr18:31514462
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46-3777T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514462 | ||||||
chr18:31514471
|
C | T | 1 | a0002c0002t0002g0096 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.46-3768C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514471 | ||||||
chr18:31514472
|
G | A | 8 | a0001c0005t0001g0284a0001c0010t0007g0282a0001c0010t0007g0285others(5): Show | 8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-3767G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514472 | ||||||
chr18:31514501
|
T | C | 1 | a0001c0006t0021g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-3738T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514501 | ||||||
chr18:31514657
|
T | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.46-3582T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514657 | ||||||
chr18:31514805
|
C | T | 14 | a0001c0003t0004g0025a0001c0003t0004g0153a0001c0003t0008g0257others(11): Show | 17 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-3434C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514805 | ||||||
chr18:31514847
|
A | G | 17 | a0001c0001t0001g0273a0001c0003t0003g0004a0001c0003t0003g0040others(14): Show | 22 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.46-3392A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31514847 | ||||||
chr18:31515126
|
A | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 199 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.46-3113A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515126 | ||||||
chr18:31515133
|
C | T | 2 | a0002c0002t0002g0101a0002c0002t0002g0105 | 2 | HG02523.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.46-3106C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515133 | ||||||
chr18:31515269
|
A | C | 2 | a0001c0003t0004g0233a0001c0003t0004g0242 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46-2970A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515269 | ||||||
chr18:31515317
|
G | C | 1 | a0001c0003t0004g0155 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.46-2922G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515317 | ||||||
chr18:31515357
|
G | A | 7 | a0001c0005t0001g0284a0001c0010t0007g0282a0001c0010t0007g0285others(4): Show | 7 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-2882G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515357 | ||||||
chr18:31515452
|
G | A | 4 | a0001c0003t0008g0254a0001c0006t0006g0251a0005c0012t0013g0252others(1): Show | 4 | HG02257.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-2787G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515452 | ||||||
chr18:31515471
|
C | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(131): Show | 160 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.46-2768C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515471 | ||||||
chr18:31515561
|
G | A | 14 | a0001c0003t0004g0025a0001c0003t0004g0153a0001c0003t0008g0257others(11): Show | 17 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-2678G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515561 | ||||||
chr18:31515822
|
A | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(137): Show | 169 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.46-2417A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515822 | ||||||
chr18:31515925
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(138): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.46-2314A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31515925 | ||||||
chr18:31516030
|
G | A | 4 | a0001c0003t0003g0032a0001c0003t0003g0190a0001c0003t0003g0246others(1): Show | 5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-2209G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516030 | ||||||
chr18:31516058
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(93): Show | 121 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.46-2181T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516058 | ||||||
chr18:31516080
|
A | C | 4 | a0001c0003t0003g0032a0001c0003t0003g0190a0001c0003t0003g0246others(1): Show | 5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-2159A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516080 | ||||||
chr18:31516126
|
CAA | C | 7 | a0001c0003t0008g0257a0001c0003t0008g0258a0001c0006t0005g0039others(4): Show | 8 | HG02055.hp1 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-2112_46-2111del others(2): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516126 | ||||||
chr18:31516141
|
G | GT | 16 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0003t0016g0166others(13): Show | 20 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.46-2088dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr18 | 31516141 | |||||
chr18:31516309
|
A | G | 1 | a0002c0004t0002g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.46-1930A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516309 | ||||||
chr18:31516310
|
C | T | 12 | a0001c0003t0003g0185a0001c0003t0004g0188a0001c0003t0016g0166others(9): Show | 17 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-1929C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516310 | ||||||
chr18:31516375
|
G | A | 7 | a0001c0005t0001g0284a0001c0010t0007g0282a0001c0010t0007g0287others(4): Show | 7 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1864G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516375 | ||||||
chr18:31516421
|
G | C | 1 | a0005c0012t0006g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-1818G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516421 | ||||||
chr18:31516427
|
A | G | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.46-1812A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516427 | ||||||
chr18:31516516
|
C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.46-1723C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516516 | ||||||
chr18:31516520
|
A | G | 1 | a0001c0003t0003g0268 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.46-1719A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516520 | ||||||
chr18:31516553
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.46-1686A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516553 | ||||||
chr18:31516646
|
G | A | 5 | a0001c0001t0009g0033a0001c0001t0009g0248a0001c0003t0004g0025others(2): Show | 7 | HG02723.hp2 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-1593G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516646 | ||||||
chr18:31516647
|
C | A | 1 | a0006c0013t0022g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.46-1592C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516647 | ||||||
chr18:31516724
|
G | A | 27 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0109others(24): Show | 33 | HG00609.hp1 HG00673.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.46-1515G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516724 | ||||||
chr18:31516858
|
C | T | 1 | a0003c0007t0002g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.46-1381C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516858 | ||||||
chr18:31516879
|
G | T | 1 | a0001c0003t0004g0025 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.46-1360G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516879 | ||||||
chr18:31516887
|
T | G | 1 | a0001c0006t0006g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46-1352T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516887 | ||||||
chr18:31516956
|
G | T | 144 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(141): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.46-1283G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516956 | ||||||
chr18:31516989
|
G | A | 1 | a0001c0006t0021g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.46-1250G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31516989 | ||||||
chr18:31517132
|
T | G | 48 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(45): Show | 54 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-1107T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517132 | ||||||
chr18:31517197
|
T | C | 1 | a0001c0003t0003g0265 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.46-1042T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517197 | ||||||
chr18:31517406
|
A | G | 2 | a0001c0003t0003g0106a0002c0002t0002g0104 | 2 | HG04184.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.46-833A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517406 | ||||||
chr18:31517506
|
A | G | 47 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(44): Show | 53 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.46-733A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517506 | ||||||
chr18:31517578
|
A | G | 46 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(43): Show | 52 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.46-661A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517578 | ||||||
chr18:31517635
|
T | G | 28 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(25): Show | 36 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.46-604T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517635 | ||||||
chr18:31517749
|
G | A | 33 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(30): Show | 42 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.46-490G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517749 | ||||||
chr18:31517772
|
G | A | 1 | a0002c0002t0002g0130 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-467G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517772 | ||||||
chr18:31517872
|
A | C | 14 | a0001c0003t0003g0185a0001c0005t0001g0006a0001c0005t0001g0145others(11): Show | 18 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.46-367A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31517872 | ||||||
chr18:31518169
|
T | C | 2 | a0001c0010t0007g0277a0001c0010t0007g0285 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.46-70T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 1/14 | chr18 | 31518169 | ||||||
chr18:31518348
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.81+74C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518348 | ||||||
chr18:31518360
|
G | A | 131 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0047others(128): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.81+86G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518360 | ||||||
chr18:31518382
|
C | T | 81 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0047others(78): Show | 100 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.81+108C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518382 | ||||||
chr18:31518510
|
C | T | 4 | a0002c0002t0002g0069a0002c0002t0002g0280a0002c0002t0002g0283others(1): Show | 4 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+236C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518510 | ||||||
chr18:31518511
|
A | G | 82 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0047others(79): Show | 100 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.81+237A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518511 | ||||||
chr18:31518539
|
C | A | 2 | a0001c0006t0006g0251a0006c0013t0012g0029 | 3 | HG03209.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.81+265C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518539 | ||||||
chr18:31518549
|
T | C | 1 | a0001c0003t0004g0250 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81+275T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518549 | ||||||
chr18:31518672
|
G | A | 224 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(221): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.81+398G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518672 | ||||||
chr18:31518714
|
T | G | 1 | a0006c0013t0022g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+440T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518714 | ||||||
chr18:31518725
|
T | TA | 78 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0047others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.81+462dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr18 | 31518725 | |||||
chr18:31518793
|
G | A | 9 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(6): Show | 9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+519G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518793 | ||||||
chr18:31518862
|
G | A | 1 | a0002c0002t0002g0060 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.81+588G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518862 | ||||||
chr18:31518895
|
A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.81+621A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31518895 | ||||||
chr18:31519121
|
T | C | 1 | a0002c0002t0002g0271 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.82-682T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31519121 | ||||||
chr18:31519324
|
A | C | 1 | a0001c0003t0004g0151 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.82-479A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31519324 | ||||||
chr18:31519634
|
C | G | 1 | a0001c0006t0005g0260 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.82-169C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 2/14 | chr18 | 31519634 | ||||||
chr18:31520134
|
C | T | 2 | a0006c0013t0012g0029a0006c0013t0022g0263 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.216+197C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520134 | ||||||
chr18:31520457
|
C | T | 5 | a0001c0010t0007g0059a0001c0010t0007g0277a0001c0010t0007g0282others(2): Show | 5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-346C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520457 | ||||||
chr18:31520470
|
C | T | 1 | a0002c0002t0002g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.217-333C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520470 | ||||||
chr18:31520714
|
G | C | 1 | a0002c0002t0002g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.217-89G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520714 | ||||||
chr18:31520738
|
C | G | 30 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(27): Show | 38 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.217-65C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520738 | ||||||
chr18:31520798
|
G | T | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.217-5G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 3/14 | chr18 | 31520798 | ||||||
chr18:31521252
|
CT | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0244a0001c0003t0004g0173others(4): Show | 7 | HG01168.hp1 HG01168.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+24delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr18 | 31521252 | |||||
chr18:31521267
|
T | A | 46 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(43): Show | 52 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.523+24T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521267 | ||||||
chr18:31521444
|
G | C | 2 | a0001c0003t0003g0117a0001c0003t0003g0142 | 2 | NA18967.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.523+201G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521444 | ||||||
chr18:31521495
|
A | G | 79 | a0001c0001t0001g0053a0001c0001t0001g0114a0001c0001t0001g0115others(76): Show | 95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.523+252A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521495 | ||||||
chr18:31521512
|
A | G | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+269A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521512 | ||||||
chr18:31521649
|
T | G | 161 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(158): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.523+406T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521649 | ||||||
chr18:31521663
|
A | G | 1 | a0006c0013t0022g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.523+420A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521663 | ||||||
chr18:31521723
|
G | A | 50 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(47): Show | 56 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.524-360G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521723 | ||||||
chr18:31521812
|
C | T | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-271C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521812 | ||||||
chr18:31521840
|
G | C | 115 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(112): Show | 140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.524-243G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521840 | ||||||
chr18:31521939
|
T | G | 1 | a0002c0002t0002g0118 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.524-144T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521939 | ||||||
chr18:31521955
|
G | A | 1 | a0001c0003t0016g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-128G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31521955 | ||||||
chr18:31522074
|
T | A | 9 | a0001c0003t0008g0254a0001c0003t0008g0257a0001c0003t0008g0258others(6): Show | 10 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.524-9T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 5/14 | chr18 | 31522074 | ||||||
chr18:31522310
|
CTTTTT | C | 31 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(28): Show | 39 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.690+62_690+66delTT others(3): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31522310 | ||||||
chr18:31522610
|
T | C | 2 | a0001c0006t0006g0179a0001c0006t0006g0180 | 2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.690+361T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31522610 | ||||||
chr18:31522950
|
G | A | 2 | a0001c0003t0004g0153a0001c0003t0004g0176 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.690+701G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31522950 | ||||||
chr18:31523018
|
G | A | 1 | a0001c0003t0003g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.690+769G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523018 | ||||||
chr18:31523101
|
A | G | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+852A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523101 | ||||||
chr18:31523124
|
G | A | 45 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(42): Show | 51 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.690+875G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523124 | ||||||
chr18:31523127
|
C | T | 2 | a0002c0002t0002g0041a0002c0002t0002g0048 | 2 | HG03704.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.690+878C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523127 | ||||||
chr18:31523172
|
C | T | 77 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(74): Show | 95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.690+923C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523172 | ||||||
chr18:31523198
|
G | A | 74 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(71): Show | 92 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.690+949G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523198 | ||||||
chr18:31523293
|
C | T | 1 | a0001c0006t0017g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690+1044C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523293 | ||||||
chr18:31523331
|
A | G | 78 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.690+1082A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523331 | ||||||
chr18:31523420
|
A | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0204a0001c0001t0001g0225 | 3 | HG01099.hp1 HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.691-1028A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523420 | ||||||
chr18:31523451
|
G | A | 1 | a0001c0006t0020g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.691-997G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523451 | ||||||
chr18:31523689
|
C | T | 13 | a0001c0003t0003g0185a0001c0005t0001g0006a0001c0005t0001g0145others(10): Show | 16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.691-759C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523689 | ||||||
chr18:31523732
|
T | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.691-716T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523732 | ||||||
chr18:31523746
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.691-702C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523746 | ||||||
chr18:31523778
|
G | A | 1 | a0005c0021t0019g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.691-670G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523778 | ||||||
chr18:31523803
|
T | C | 43 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0004g0025others(40): Show | 48 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.691-645T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523803 | ||||||
chr18:31523807
|
G | A | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-641G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31523807 | ||||||
chr18:31524092
|
C | T | 72 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(69): Show | 85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.691-356C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524092 | ||||||
chr18:31524172
|
A | G | 29 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(26): Show | 37 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.691-276A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524172 | ||||||
chr18:31524241
|
G | A | 78 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.691-207G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524241 | ||||||
chr18:31524245
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0162a0001c0001t0001g0165others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-203A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524245 | ||||||
chr18:31524258
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.691-190G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524258 | ||||||
chr18:31524301
|
T | C | 72 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(69): Show | 85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.691-147T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524301 | ||||||
chr18:31524365
|
C | T | 6 | a0001c0003t0004g0209a0002c0004t0002g0036a0002c0004t0002g0037others(3): Show | 8 | HG00673.hp2 HG03486.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-83C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 6/14 | chr18 | 31524365 | ||||||
chr18:31524601
|
C | A | 74 | a0001c0006t0006g0179a0001c0006t0006g0180a0002c0002t0002g0002others(71): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.828+16C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 7/14 | chr18 | 31524601 | ||||||
chr18:31524915
|
G | A | 77 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(74): Show | 94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1014+27G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31524915 | ||||||
chr18:31524939
|
G | A | 1 | a0001c0003t0016g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1014+51G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31524939 | ||||||
chr18:31524998
|
G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1014+110G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31524998 | ||||||
chr18:31525010
|
T | C | 1 | a0002c0002t0002g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1014+122T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525010 | ||||||
chr18:31525107
|
G | T | 13 | a0001c0003t0003g0185a0001c0005t0001g0006a0001c0005t0001g0145others(10): Show | 16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1014+219G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525107 | ||||||
chr18:31525154
|
T | C | 36 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0030others(33): Show | 41 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1014+266T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525154 | ||||||
chr18:31525213
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1014+325T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525213 | ||||||
chr18:31525289
|
G | A | 2 | a0001c0006t0006g0170a0001c0006t0017g0163 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1014+401G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525289 | ||||||
chr18:31525536
|
G | A | 11 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(8): Show | 12 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+648G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525536 | ||||||
chr18:31525612
|
G | A | 1 | a0001c0011t0003g0226 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1014+724G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525612 | ||||||
chr18:31525918
|
G | A | 78 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1014+1030G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525918 | ||||||
chr18:31525933
|
G | A | 1 | a0001c0003t0003g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1014+1045G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525933 | ||||||
chr18:31525999
|
C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1014+1111C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31525999 | ||||||
chr18:31526091
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0049 | 3 | HG00735.hp1 HG02129.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1014+1203C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526091 | ||||||
chr18:31526157
|
A | G | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1014+1269A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526157 | ||||||
chr18:31526293
|
C | T | 5 | a0001c0010t0007g0059a0001c0010t0007g0277a0001c0010t0007g0282others(2): Show | 5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014+1405C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526293 | ||||||
chr18:31526379
|
C | T | 83 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(80): Show | 97 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1014+1491C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526379 | ||||||
chr18:31526603
|
G | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0162a0001c0001t0001g0165others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+1715G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526603 | ||||||
chr18:31526649
|
G | A | 1 | a0007c0015t0011g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1014+1761G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526649 | ||||||
chr18:31526649
|
G | T | 77 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(74): Show | 94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1014+1761G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526649 | ||||||
chr18:31526677
|
A | G | 1 | a0005c0021t0019g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1014+1789A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526677 | ||||||
chr18:31526724
|
T | G | 1 | a0001c0003t0003g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1014+1836T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526724 | ||||||
chr18:31526762
|
G | A | 1 | a0001c0005t0001g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1014+1874G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526762 | ||||||
chr18:31526858
|
G | A | 77 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(74): Show | 94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1014+1970G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526858 | ||||||
chr18:31526935
|
T | A | 78 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1014+2047T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31526935 | ||||||
chr18:31527491
|
G | A | 52 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(49): Show | 61 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1014+2603G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527491 | ||||||
chr18:31527583
|
C | T | 9 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(6): Show | 9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+2695C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527583 | ||||||
chr18:31527628
|
C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1014+2740C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527628 | ||||||
chr18:31527651
|
A | T | 77 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(74): Show | 94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1014+2763A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527651 | ||||||
chr18:31527693
|
T | C | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1014+2805T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527693 | ||||||
chr18:31527749
|
A | G | 2 | a0001c0005t0001g0171a0001c0005t0001g0284 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1014+2861A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527749 | ||||||
chr18:31527767
|
T | G | 164 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(161): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1014+2879T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527767 | ||||||
chr18:31527840
|
G | A | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+2952G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527840 | ||||||
chr18:31527854
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0195 | 2 | NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1014+2966C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527854 | ||||||
chr18:31527887
|
G | A | 4 | a0005c0012t0006g0133a0005c0012t0013g0252a0005c0012t0013g0255others(1): Show | 4 | HG02257.hp1 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+2999G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527887 | ||||||
chr18:31527928
|
G | A | 1 | a0001c0005t0001g0184 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014+3040G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527928 | ||||||
chr18:31527975
|
T | C | 1 | a0001c0003t0004g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1015-3012T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31527975 | ||||||
chr18:31528119
|
A | T | 9 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(6): Show | 9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-2868A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528119 | ||||||
chr18:31528124
|
G | A | 78 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1015-2863G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528124 | ||||||
chr18:31528157
|
A | G | 1 | a0013c0026t0005g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1015-2830A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528157 | ||||||
chr18:31528195
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1015-2792G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528195 | ||||||
chr18:31528418
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1015-2569C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528418 | ||||||
chr18:31528437
|
C | T | 1 | a0005c0012t0013g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-2550C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528437 | ||||||
chr18:31528438
|
A | G | 166 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(163): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1015-2549A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528438 | ||||||
chr18:31528498
|
G | A | 13 | a0001c0003t0003g0185a0001c0005t0001g0006a0001c0005t0001g0145others(10): Show | 16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1015-2489G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528498 | ||||||
chr18:31528542
|
A | T | 172 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(169): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1015-2445A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528542 | ||||||
chr18:31528554
|
C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1015-2433C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528554 | ||||||
chr18:31528613
|
A | G | 78 | a0001c0003t0016g0166a0001c0006t0006g0027a0001c0006t0006g0170others(75): Show | 95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1015-2374A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528613 | ||||||
chr18:31528626
|
CCTGAACC others(214): Show |
C | 1 | a0001c0001t0001g0234 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1015-2358_1015-213 others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31528626 | |||||
chr18:31528709
|
C | CA | 20 | a0001c0001t0009g0248a0001c0003t0003g0142a0001c0003t0003g0193others(17): Show | 23 | HG00140.hp2 HG00544.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1015-2259dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31528709 | |||||
chr18:31528709
|
CA | C | 9 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0005t0001g0213others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1015-2259delA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31528709 | |||||
chr18:31528743
|
T | C | 87 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(84): Show | 101 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1015-2244T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528743 | ||||||
chr18:31528774
|
A | G | 1 | a0002c0002t0002g0286 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1015-2213A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528774 | ||||||
chr18:31528963
|
C | G | 3 | a0001c0003t0004g0026a0001c0003t0004g0148a0001c0003t0004g0150 | 4 | HG02165.hp2 NA19000.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-2024C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31528963 | ||||||
chr18:31529000
|
A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1015-1987A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529000 | ||||||
chr18:31529073
|
A | G | 171 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(168): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1015-1914A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529073 | ||||||
chr18:31529172
|
A | C | 12 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(9): Show | 13 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-1815A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529172 | ||||||
chr18:31529336
|
A | T | 2 | a0001c0006t0006g0170a0001c0006t0017g0163 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1015-1651A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529336 | ||||||
chr18:31529483
|
A | G | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-1504A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529483 | ||||||
chr18:31529679
|
C | A | 87 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(84): Show | 101 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1015-1308C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31529679 | ||||||
chr18:31530155
|
G | A | 1 | a0001c0025t0001g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1015-832G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530155 | ||||||
chr18:31530350
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1015-637A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530350 | ||||||
chr18:31530363
|
A | T | 17 | a0002c0004t0002g0012a0002c0004t0002g0016a0002c0004t0002g0023others(14): Show | 22 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1015-624A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530363 | ||||||
chr18:31530517
|
A | G | 13 | a0001c0003t0003g0185a0001c0005t0001g0006a0001c0005t0001g0145others(10): Show | 16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1015-470A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530517 | ||||||
chr18:31530545
|
G | A | 3 | a0001c0006t0006g0251a0006c0013t0012g0029a0006c0013t0022g0263 | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-442G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530545 | ||||||
chr18:31530619
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1015-368A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530619 | ||||||
chr18:31530721
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1015-266A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530721 | ||||||
chr18:31530807
|
C | A | 13 | a0001c0003t0003g0185a0001c0005t0001g0006a0001c0005t0001g0145others(10): Show | 16 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1015-180C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | chr18 | 31530807 | ||||||
chr18:31530915
|
CATGTAT | C | 3 | a0001c0006t0006g0251a0006c0013t0012g0029a0006c0013t0022g0263 | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-58_1015-53del others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr18 | 31530915 | |||||
chr18:31531401
|
G | A | 34 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0030others(31): Show | 39 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1280+149G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531401 | ||||||
chr18:31531486
|
A | G | 90 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(87): Show | 109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1280+234A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531486 | ||||||
chr18:31531539
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0092 | 2 | HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1280+287C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531539 | ||||||
chr18:31531694
|
G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+442G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531694 | ||||||
chr18:31531702
|
C | T | 12 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161others(9): Show | 13 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1280+450C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531702 | ||||||
chr18:31531916
|
G | A | 3 | a0002c0004t0002g0023a0002c0004t0002g0071a0002c0004t0002g0279 | 4 | HG02083.hp2 HG02129.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280+664G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531916 | ||||||
chr18:31531918
|
C | T | 5 | a0001c0006t0021g0182a0005c0012t0006g0133a0005c0012t0013g0252others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+666C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31531918 | ||||||
chr18:31532143
|
T | C | 1 | a0001c0003t0003g0269 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1280+891T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532143 | ||||||
chr18:31532178
|
G | A | 3 | a0001c0003t0003g0193a0001c0003t0003g0215a0001c0003t0015g0161 | 3 | HG02630.hp2 HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1280+926G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532178 | ||||||
chr18:31532215
|
G | A | 3 | a0001c0006t0006g0251a0006c0013t0012g0029a0006c0013t0022g0263 | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280+963G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532215 | ||||||
chr18:31532250
|
G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+998G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532250 | ||||||
chr18:31532315
|
A | G | 12 | a0001c0005t0001g0006a0001c0005t0001g0145a0001c0005t0001g0146others(9): Show | 15 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1280+1063A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532315 | ||||||
chr18:31532477
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1280+1225T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532477 | ||||||
chr18:31532500
|
C | T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+1248C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532500 | ||||||
chr18:31532610
|
T | C | 10 | a0001c0003t0003g0185a0001c0003t0003g0193a0001c0003t0003g0215others(7): Show | 10 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1280+1358T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532610 | ||||||
chr18:31532697
|
G | A | 1 | a0001c0005t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1280+1445G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532697 | ||||||
chr18:31532767
|
T | A | 5 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+1515T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532767 | ||||||
chr18:31532778
|
T | C | 4 | a0005c0012t0006g0133a0005c0012t0013g0252a0005c0012t0013g0255others(1): Show | 4 | HG02257.hp1 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280+1526T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532778 | ||||||
chr18:31532850
|
A | G | 5 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+1598A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532850 | ||||||
chr18:31532903
|
G | A | 12 | a0001c0003t0003g0185a0001c0003t0003g0193a0001c0003t0003g0215others(9): Show | 13 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1280+1651G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31532903 | ||||||
chr18:31532904
|
CTGTTT | C | 3 | a0001c0003t0004g0191a0001c0003t0004g0210a0001c0003t0004g0250 | 3 | HG01884.hp1 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1280+1658_1280+166 others(9): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532904 | |||||
chr18:31532907
|
T | TTTTG | 21 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0001t0001g0241others(18): Show | 22 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1280+1683_1280+168 others(8): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | |||||
chr18:31532907
|
T | TTTTGTTT others(1): Show |
4 | a0001c0006t0005g0039a0001c0006t0005g0253a0001c0006t0005g0256others(1): Show | 5 | HG02055.hp1 HG02886.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+1679_1280+168 others(12): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | |||||
chr18:31532907
|
TTTTG | T | 12 | a0001c0003t0003g0185a0001c0003t0003g0193a0001c0003t0003g0215others(9): Show | 12 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1280+1683_1280+168 others(8): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | |||||
chr18:31532907
|
TTTTGTTT others(1): Show |
T | 97 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0003t0003g0275others(94): Show | 119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1280+1679_1280+168 others(12): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | |||||
chr18:31532907
|
TTTTGTTT others(5): Show |
T | 1 | a0006c0013t0012g0029 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1280+1675_1280+168 others(16): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | |||||
chr18:31532907
|
TTTTGTTT others(9): Show |
T | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1280+1671_1280+168 others(20): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31532907 | |||||
chr18:31533045
|
A | T | 1 | a0005c0012t0013g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1280+1793A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533045 | ||||||
chr18:31533311
|
A | C | 1 | a0002c0002t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1281-1959A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533311 | ||||||
chr18:31533314
|
A | T | 1 | a0001c0001t0001g0014 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1281-1956A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533314 | ||||||
chr18:31533512
|
A | C | 1 | a0002c0002t0002g0096 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1281-1758A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533512 | ||||||
chr18:31533698
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0195 | 2 | NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1281-1572T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31533698 | ||||||
chr18:31533991
|
C | CT | 37 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(34): Show | 45 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1281-1262dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | |||||
chr18:31533991
|
C | CTT | 26 | a0001c0003t0003g0142a0001c0003t0004g0025a0001c0003t0004g0026others(23): Show | 31 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1281-1263_1281-126 others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | |||||
chr18:31533991
|
C | CTTT | 6 | a0001c0003t0004g0097a0001c0003t0004g0116a0001c0003t0004g0151others(3): Show | 6 | HG02074.hp1 HG04184.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-1264_1281-126 others(7): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | |||||
chr18:31533991
|
CT | C | 98 | a0001c0001t0001g0051a0001c0001t0001g0198a0001c0001t0001g0205others(95): Show | 119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1281-1262delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31533991 | |||||
chr18:31534186
|
A | C | 115 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0003t0003g0185others(112): Show | 139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1281-1084A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534186 | ||||||
chr18:31534194
|
G | A | 1 | a0005c0012t0006g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1281-1076G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534194 | ||||||
chr18:31534236
|
A | C | 1 | a0002c0002t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1281-1034A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534236 | ||||||
chr18:31534248
|
G | A | 95 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(92): Show | 118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1281-1022G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534248 | ||||||
chr18:31534441
|
A | C | 1 | a0001c0001t0001g0243 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1281-829A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534441 | ||||||
chr18:31534479
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1281-791G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534479 | ||||||
chr18:31534508
|
A | AT | 18 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0199others(15): Show | 19 | HG00741.hp1 HG02015.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281-742dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | |||||
chr18:31534508
|
A | ATT | 78 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(75): Show | 94 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1281-743_1281-742d others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | |||||
chr18:31534508
|
A | ATTTTT | 83 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0006t0006g0027others(80): Show | 104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1281-746_1281-742d others(7): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | |||||
chr18:31534508
|
A | ATTTTTT | 11 | a0001c0006t0006g0179a0002c0002t0002g0056a0002c0002t0002g0060others(8): Show | 12 | HG00621.hp2 HG02056.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281-747_1281-742d others(8): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | |||||
chr18:31534508
|
AT | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0092others(4): Show | 7 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1281-742delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | |||||
chr18:31534508
|
ATT | A | 5 | a0001c0006t0005g0039a0001c0006t0005g0253a0001c0006t0005g0256others(2): Show | 6 | HG02055.hp1 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281-743_1281-742d others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr18 | 31534508 | |||||
chr18:31534533
|
T | C | 115 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0003t0003g0185others(112): Show | 139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1281-737T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534533 | ||||||
chr18:31534580
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1281-690G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534580 | ||||||
chr18:31534589
|
C | T | 96 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0006t0006g0027others(93): Show | 118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1281-681C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534589 | ||||||
chr18:31534657
|
C | T | 5 | a0001c0010t0007g0059a0001c0010t0007g0277a0001c0010t0007g0282others(2): Show | 5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281-613C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534657 | ||||||
chr18:31534658
|
G | A | 94 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(91): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1281-612G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534658 | ||||||
chr18:31534691
|
G | A | 3 | a0001c0006t0006g0251a0006c0013t0012g0029a0006c0013t0022g0263 | 4 | HG02922.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-579G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534691 | ||||||
chr18:31534800
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1281-470G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31534800 | ||||||
chr18:31535198
|
A | C | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1281-72A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 9/14 | chr18 | 31535198 | ||||||
chr18:31535701
|
G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1423+289G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535701 | ||||||
chr18:31535739
|
T | G | 1 | a0001c0001t0001g0243 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1423+327T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535739 | ||||||
chr18:31535740
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1423+328C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535740 | ||||||
chr18:31535774
|
A | C | 1 | a0003c0007t0002g0231 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1423+362A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535774 | ||||||
chr18:31535781
|
C | A | 1 | a0002c0002t0002g0104 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1423+369C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535781 | ||||||
chr18:31535947
|
T | A | 190 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0003t0003g0004others(187): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1424-255T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 10/14 | chr18 | 31535947 | ||||||
chr18:31536499
|
T | C | 47 | a0001c0003t0003g0215a0001c0003t0004g0025a0001c0003t0004g0026others(44): Show | 54 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.1651+70T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536499 | ||||||
chr18:31536717
|
G | A | 1 | a0001c0006t0006g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1651+288G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536717 | ||||||
chr18:31536837
|
T | C | 6 | a0001c0001t0001g0198a0001c0001t0001g0221a0002c0004t0002g0012others(3): Show | 7 | HG00609.hp2 HG02155.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1651+408T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536837 | ||||||
chr18:31536936
|
CAG | C | 2 | a0006c0013t0012g0029a0006c0013t0022g0263 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1651+508_1651+509d others(4): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31536936 | ||||||
chr18:31537150
|
GT | G | 93 | a0001c0001t0001g0198a0001c0001t0001g0221a0002c0002t0002g0002others(90): Show | 114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1651+731delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr18 | 31537150 | |||||
chr18:31537152
|
T | G | 1 | a0003c0007t0002g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1651+723T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537152 | ||||||
chr18:31537186
|
C | G | 2 | a0006c0013t0012g0029a0006c0013t0022g0263 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1651+757C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537186 | ||||||
chr18:31537219
|
T | A | 2 | a0001c0005t0001g0167a0001c0005t0001g0169 | 2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1651+790T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537219 | ||||||
chr18:31537236
|
A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1651+807A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537236 | ||||||
chr18:31537418
|
G | A | 91 | a0001c0001t0001g0198a0001c0001t0001g0221a0002c0002t0002g0002others(88): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1651+989G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537418 | ||||||
chr18:31537447
|
G | A | 46 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0030others(43): Show | 53 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1651+1018G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537447 | ||||||
chr18:31537480
|
G | A | 1 | a0002c0027t0002g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1651+1051G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537480 | ||||||
chr18:31537492
|
A | G | 91 | a0001c0001t0001g0198a0001c0001t0001g0221a0002c0002t0002g0002others(88): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1651+1063A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537492 | ||||||
chr18:31537537
|
T | C | 91 | a0001c0001t0001g0198a0001c0001t0001g0221a0002c0002t0002g0002others(88): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1651+1108T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537537 | ||||||
chr18:31537546
|
A | G | 183 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0003t0003g0004others(180): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1651+1117A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537546 | ||||||
chr18:31537558
|
G | T | 4 | a0002c0002t0002g0069a0002c0002t0002g0280a0002c0002t0002g0283others(1): Show | 4 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651+1129G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537558 | ||||||
chr18:31537597
|
T | C | 138 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0003t0004g0025others(135): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1652-1154T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537597 | ||||||
chr18:31537794
|
G | A | 1 | a0001c0003t0003g0281 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1652-957G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537794 | ||||||
chr18:31537836
|
C | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1652-915C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537836 | ||||||
chr18:31537898
|
G | A | 91 | a0001c0001t0001g0198a0001c0001t0001g0221a0002c0002t0002g0002others(88): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1652-853G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537898 | ||||||
chr18:31537923
|
G | A | 2 | a0005c0012t0006g0133a0005c0021t0019g0164 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1652-828G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537923 | ||||||
chr18:31537989
|
A | T | 1 | a0001c0005t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1652-762A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537989 | ||||||
chr18:31537993
|
C | T | 1 | a0001c0005t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1652-758C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31537993 | ||||||
chr18:31538110
|
T | TA | 41 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0030others(38): Show | 47 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1652-633dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr18 | 31538110 | |||||
chr18:31538298
|
C | T | 1 | a0001c0003t0016g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1652-453C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538298 | ||||||
chr18:31538316
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1652-435G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538316 | ||||||
chr18:31538343
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1652-408G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538343 | ||||||
chr18:31538393
|
G | GT | 38 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0030others(35): Show | 43 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1652-349dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr18 | 31538393 | |||||
chr18:31538397
|
T | A | 1 | a0002c0002t0002g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1652-354T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538397 | ||||||
chr18:31538402
|
T | A | 1 | a0002c0002t0002g0042 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1652-349T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538402 | ||||||
chr18:31538585
|
G | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1652-166G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538585 | ||||||
chr18:31538714
|
G | A | 2 | a0001c0006t0006g0170a0001c0006t0017g0163 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1652-37G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 11/14 | chr18 | 31538714 | ||||||
chr18:31539040
|
G | A | 1 | a0001c0003t0003g0126 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1879+62G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539040 | ||||||
chr18:31539082
|
C | T | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1879+104C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539082 | ||||||
chr18:31539155
|
C | T | 1 | a0001c0010t0007g0287 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1879+177C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539155 | ||||||
chr18:31539295
|
T | C | 87 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(84): Show | 102 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1879+317T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539295 | ||||||
chr18:31539322
|
A | C | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1879+344A>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539322 | ||||||
chr18:31539394
|
T | C | 182 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(179): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1879+416T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539394 | ||||||
chr18:31539527
|
C | T | 28 | a0001c0003t0003g0004a0001c0003t0003g0040a0001c0003t0003g0077others(25): Show | 35 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1879+549C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539527 | ||||||
chr18:31539579
|
C | T | 1 | a0004c0009t0003g0093 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1879+601C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539579 | ||||||
chr18:31539601
|
C | A | 1 | a0001c0006t0020g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1879+623C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539601 | ||||||
chr18:31539750
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1879+772C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539750 | ||||||
chr18:31539825
|
A | G | 1 | a0001c0006t0006g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1879+847A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31539825 | ||||||
chr18:31540020
|
T | A | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1879+1042T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540020 | ||||||
chr18:31540236
|
A | G | 2 | a0002c0002t0002g0206a0002c0002t0002g0219 | 2 | NA18959.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1880-957A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540236 | ||||||
chr18:31540446
|
C | T | 89 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0017others(86): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1880-747C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540446 | ||||||
chr18:31540474
|
C | G | 89 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0017others(86): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1880-719C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540474 | ||||||
chr18:31540567
|
G | A | 89 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0017others(86): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1880-626G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540567 | ||||||
chr18:31540576
|
G | A | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1880-617G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540576 | ||||||
chr18:31540612
|
G | A | 6 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1880-581G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540612 | ||||||
chr18:31540812
|
C | T | 2 | a0005c0012t0013g0252a0005c0012t0013g0255 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1880-381C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540812 | ||||||
chr18:31540840
|
A | AT | 33 | a0001c0003t0004g0025a0001c0003t0004g0026a0001c0003t0004g0030others(30): Show | 38 | HG00140.hp2 HG00609.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1880-344dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr18 | 31540840 | |||||
chr18:31540845
|
T | G | 1 | a0001c0008t0002g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1880-348T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540845 | ||||||
chr18:31540912
|
T | C | 77 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(74): Show | 90 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1880-281T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 12/14 | chr18 | 31540912 | ||||||
chr18:31541525
|
C | T | 89 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0017others(86): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2001+211C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541525 | ||||||
chr18:31541558
|
G | C | 89 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0017others(86): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2001+244G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541558 | ||||||
chr18:31541622
|
C | T | 14 | a0001c0005t0001g0006a0001c0005t0001g0145a0001c0005t0001g0146others(11): Show | 17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2001+308C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541622 | ||||||
chr18:31541649
|
T | G | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2001+335T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541649 | ||||||
chr18:31541800
|
C | A | 89 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0017others(86): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2001+486C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541800 | ||||||
chr18:31541866
|
C | A | 6 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001+552C>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541866 | ||||||
chr18:31541933
|
T | A | 85 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(82): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2002-587T>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541933 | ||||||
chr18:31541977
|
TG | T | 14 | a0001c0005t0001g0006a0001c0005t0001g0145a0001c0005t0001g0146others(11): Show | 17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2002-542delG | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31541977 | ||||||
chr18:31542023
|
C | T | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2002-497C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542023 | ||||||
chr18:31542304
|
T | C | 6 | a0001c0006t0005g0039a0001c0006t0005g0253a0001c0006t0005g0256others(3): Show | 7 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-216T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542304 | ||||||
chr18:31542325
|
T | C | 2 | a0001c0005t0001g0212a0001c0005t0001g0213 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2002-195T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542325 | ||||||
chr18:31542385
|
A | G | 6 | a0001c0006t0005g0039a0001c0006t0005g0253a0001c0006t0005g0256others(3): Show | 7 | HG02055.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002-135A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 13/14 | chr18 | 31542385 | ||||||
chr18:31542959
|
GT | G | 93 | a0001c0003t0003g0265a0001c0003t0008g0254a0001c0006t0006g0027others(90): Show | 115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2334+121delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31542959 | |||||
chr18:31542987
|
A | G | 3 | a0001c0006t0021g0182a0005c0012t0013g0252a0005c0012t0013g0255 | 3 | HG01884.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2334+135A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31542987 | ||||||
chr18:31543351
|
G | T | 1 | a0002c0002t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2334+499G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543351 | ||||||
chr18:31543368
|
T | G | 14 | a0001c0005t0001g0006a0001c0005t0001g0145a0001c0005t0001g0146others(11): Show | 17 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2334+516T>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543368 | ||||||
chr18:31543371
|
G | A | 1 | a0001c0014t0001g0228 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2334+519G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543371 | ||||||
chr18:31543459
|
G | T | 2 | a0005c0012t0006g0133a0005c0021t0019g0164 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2334+607G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543459 | ||||||
chr18:31543462
|
A | G | 1 | a0001c0006t0006g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2334+610A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543462 | ||||||
chr18:31543500
|
A | G | 2 | a0005c0012t0006g0133a0005c0021t0019g0164 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2334+648A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543500 | ||||||
chr18:31543516
|
G | A | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2334+664G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543516 | ||||||
chr18:31543615
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2334+763C>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543615 | ||||||
chr18:31543796
|
G | A | 3 | a0001c0003t0008g0254a0001c0003t0008g0257a0001c0003t0008g0258 | 3 | HG02109.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2334+944G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543796 | ||||||
chr18:31543861
|
G | A | 39 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(36): Show | 47 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.2334+1009G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543861 | ||||||
chr18:31543864
|
T | TA | 96 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0128others(93): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2334+1032dupA | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31543864 | |||||
chr18:31543864
|
T | TAA | 14 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0017g0163others(11): Show | 17 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2334+1031_2334+103 others(6): Show |
DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31543864 | |||||
chr18:31543892
|
A | G | 5 | a0001c0010t0007g0059a0001c0010t0007g0277a0001c0010t0007g0282others(2): Show | 5 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2334+1040A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543892 | ||||||
chr18:31543973
|
A | G | 1 | a0001c0003t0004g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2334+1121A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31543973 | ||||||
chr18:31544104
|
G | C | 95 | a0001c0008t0002g0064a0001c0008t0002g0074a0001c0008t0002g0083others(92): Show | 116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2334+1252G>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544104 | ||||||
chr18:31544147
|
A | T | 1 | a0002c0002t0002g0060 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2334+1295A>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544147 | ||||||
chr18:31544404
|
G | A | 3 | a0005c0012t0006g0133a0005c0021t0019g0164a0009c0024t0018g0175 | 3 | HG01243.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2335-1317G>A | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544404 | ||||||
chr18:31544461
|
C | T | 105 | a0001c0006t0006g0027a0001c0006t0006g0170a0001c0006t0006g0179others(102): Show | 128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2335-1260C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544461 | ||||||
chr18:31544487
|
A | G | 1 | a0002c0016t0010g0011 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2335-1234A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544487 | ||||||
chr18:31544748
|
T | C | 72 | a0001c0003t0003g0004a0001c0003t0003g0032a0001c0003t0003g0040others(69): Show | 85 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2335-973T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544748 | ||||||
chr18:31544769
|
T | C | 1 | a0001c0003t0004g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2335-952T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544769 | ||||||
chr18:31544859
|
A | G | 2 | a0007c0015t0011g0261a0007c0015t0011g0264 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2335-862A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544859 | ||||||
chr18:31544901
|
A | G | 8 | a0001c0006t0020g0081a0001c0010t0007g0059a0001c0010t0007g0277others(5): Show | 9 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2335-820A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544901 | ||||||
chr18:31544947
|
C | T | 2 | a0001c0006t0006g0170a0001c0006t0017g0163 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2335-774C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31544947 | ||||||
chr18:31545014
|
G | T | 2 | a0006c0013t0012g0029a0006c0013t0022g0263 | 3 | HG02922.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2335-707G>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545014 | ||||||
chr18:31545097
|
C | T | 1 | a0001c0005t0001g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2335-624C>T | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545097 | ||||||
chr18:31545178
|
T | C | 2 | a0005c0012t0006g0133a0005c0021t0019g0164 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2335-543T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545178 | ||||||
chr18:31545274
|
A | G | 2 | a0005c0012t0013g0252a0005c0012t0013g0255 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2335-447A>G | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545274 | ||||||
chr18:31545457
|
T | C | 1 | a0002c0002t0002g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2335-264T>C | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | chr18 | 31545457 | ||||||
chr18:31545515
|
A | AT | 7 | a0001c0005t0001g0169a0001c0006t0005g0039a0001c0006t0005g0253others(4): Show | 8 | HG02055.hp1 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335-200dupT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31545515 | |||||
chr18:31545687
|
GT | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0181a0001c0014t0001g0214others(1): Show | 4 | HG02809.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2335-30delT | DSG2 | ENSG00000046604.14 | transcript | ENST00000261590.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr18 | 31545687 |